Showing results (1-10 of 69) with videos related to

Sort By:
Pageof 7
Gene|July 31, 2012
15q11.2 microdeletion and FMR1 premutation in a family with intellectual disabilities and autismIrene Madrigal, Laia Rodríguez-Revenga, Mar Xunclà, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
Trisomy of 19.4 Mb region of chromosome 22 and subtelomeric 17p identified in a male without clinical affectationCarme Morales, Anna Soler, Ester Margarit, et al.
Journal of Clinical Medicine|August 29, 2024
Prenatal Screening of Chromosomal Anomalies Using Genome-Wide or Target Cell-Free DNA: Preferences and Satisfaction of Pregnant WomenVictoria Ardiles-Ruesjas, Roser Viñals, Montse Pauta, et al.
Psychiatric Genetics|July 17, 2008
Evidence of depressive symptoms in fragile-X syndrome premutated femalesLaia Rodriguez-Revenga, Irene Madrigal, Montserrat Alegret, et al.
American Journal of Medical Genetics. Part A|April 11, 2012
12p13 rearrangements: 6 Mb deletion responsible for ID/MCA and reciprocal duplication without clinical responsibilityIrene Madrigal, Margarita Martinez, Laia Rodriguez-Revenga, et al.
Fetal Diagnosis and Therapy|September 9, 2020
Cell-Free DNA Testing: What Is the Reason Why High-Risk Women Choose It?Leticia Benítez-Quintanilla, Montse Pauta, Isabel Matas, et al.
Genomics|February 16, 2010
Identification of human specific gene duplications relative to other primates by array CGH and quantitative PCRGemma Armengol, Sakari Knuutila, Juan-José Lozano, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|October 26, 2010
Protocol proposal for Friedreich ataxia molecular diagnosis using fluorescent and triplet repeat primed polymerase chain reactionMar Xunclà, Laia Rodríguez-Revenga, Irene Madrigal, et al.
Pageof 7